Pharmacological chaperone-mediated in vivo folding and stabilization of the P23H-opsin mutant associated with autosomal dominant retinitis pigmentosa (Q34338708)

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English	Pharmacological chaperone-mediated in vivo folding and stabilization of the P23H-opsin mutant associated with autosomal dominant retinitis pigmentosa	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

1 August 2017

Pharmacological chaperone-mediated in vivo folding and stabilization of the P23H-opsin mutant associated with autosomal dominant retinitis pigmentosa (English)

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Europe PubMed Central

PubMed publication ID

1 August 2017

molecular chaperones

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1 reference

based on heuristic

inferred from title

retinitis pigmentosa

1 reference

based on heuristic

inferred from title

Slawomir Filipek

5

object named as

Sławomir Filipek

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Europe PubMed Central

PubMed publication ID

1 August 2017

Krzysztof Palczewski

6

object named as

Krzysztof Palczewski

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Europe PubMed Central

PubMed publication ID

1 August 2017

Yoshikazu Imanishi

3

object named as

Yoshikazu Imanishi

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1 August 2017

author name string

Syed M Noorwez

1

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PubMed publication ID

1 August 2017

Vladimir Kuksa

2

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1 August 2017

Li Zhu

4

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1 August 2017

Shalesh Kaushal

7

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1 August 2017

language of work or name

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publication date

1 February 2003

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1 August 2017

Journal of Biological Chemistry

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1 August 2017

278

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1 August 2017

16

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Europe PubMed Central

PubMed publication ID

1 August 2017

14442-14450

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Europe PubMed Central

PubMed publication ID

1 August 2017

G protein-coupled receptor drug discovery: implications from the crystal structure of rhodopsin.

1 reference

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6 July 2018

G protein-coupled receptor rhodopsin: a prospectus

1 reference

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6 July 2018

Biochemical and physiological properties of rhodopsin regenerated with 11-cis-6-ring- and 7-ring-retinals

1 reference

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6 July 2018

The cellular fate of mutant rhodopsin: quality control, degradation and aggresome formation.

1 reference

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Recovery of visual functions in a mouse model of Leber congenital amaurosis

1 reference

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Requirement of an intact microtubule cytoskeleton for aggregation and inclusion body formation by a mutant huntingtin fragment.

1 reference

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6 July 2018

Isomerization of 11-cis-retinoids to all-trans-retinoids in vitro and in vivo

1 reference

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Unfolding retinal dystrophies: a role for molecular chaperones?

1 reference

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6 July 2018

Crystal structure of rhodopsin: implications for vision and beyond

1 reference

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Advances in Determination of a High-Resolution Three-Dimensional Structure of Rhodopsin, a Model of G-Protein-Coupled Receptors (GPCRs)

1 reference

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6 July 2018

Protein misfolding and disease; protein refolding and therapy

1 reference

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Activation of rhodopsin: new insights from structural and biochemical studies

1 reference

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6 July 2018

Mechanism of rhodopsin activation as examined with ring-constrained retinal analogs and the crystal structure of the ground state protein

1 reference

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Conformational and temperature-sensitive stability defects of the delta F508 cystic fibrosis transmembrane conductance regulator in post-endoplasmic reticulum compartments.

1 reference

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Crystal structure of rhodopsin: A G protein-coupled receptor

1 reference

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X-Ray diffraction analysis of three-dimensional crystals of bovine rhodopsin obtained from mixed micelles.

1 reference

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6 July 2018

Molecular genetics of human retinal disease

1 reference

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6 July 2018

Chemical chaperones mediate increased secretion of mutant alpha 1-antitrypsin (alpha 1-AT) Z: A potential pharmacological strategy for prevention of liver injury and emphysema in alpha 1-AT deficiency

1 reference

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1 reference

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Effect of vitamin A supplementation on rhodopsin mutants threonine-17 --> methionine and proline-347 --> serine in transgenic mice and in cell cultures

1 reference

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1 reference

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Synthesis and characterization of a novel retinylamine analog inhibitor of constitutively active rhodopsin mutants found in patients with autosomal dominant retinitis pigmentosa

1 reference

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6 July 2018

Rhodopsin mutations responsible for autosomal dominant retinitis pigmentosa. Clustering of functional classes along the polypeptide chain

1 reference

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6 July 2018

Structure and function in rhodopsin. 7. Point mutations associated with autosomal dominant retinitis pigmentosa

1 reference

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6 July 2018

Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness

1 reference

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Structure and function in rhodopsin. Separation and characterization of the correctly folded and misfolded opsins produced on expression of an opsin mutant gene containing only the native intradiscal cysteine codons

1 reference

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1 reference

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A rhodopsin mutant linked to autosomal dominant retinitis pigmentosa is prone to aggregate and interacts with the ubiquitin proteasome system

1 reference

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1 reference

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A mouse model to test the in vivo efficacy of chemical chaperones

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https://pubmed.ncbi.nlm.nih.gov/12566452

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inferred from PubMed ID database lookup

Pharmacological rescue of mutant p53 conformation and function

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https://pubmed.ncbi.nlm.nih.gov/12566452

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Reversion of prion protein conformational changes by synthetic b-sheet breaker peptides

1 reference

https://pubmed.ncbi.nlm.nih.gov/12566452

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Synthetic retinals: convenient probes of rhodopsin and visual transduction process

1 reference

https://pubmed.ncbi.nlm.nih.gov/12566452

12 December 2020

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Animal models of inherited retinal diseases

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inferred from PubMed ID database lookup

Identifiers

10.1074/JBC.M300087200

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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